NDC 73377-031-01 - Mebendazole

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 73377-031
Requested NDC: 73377-031-01
Package NDCs from labels: 73377-031-01
Manufacturer: AX Pharmaceutical Corp | SOLARA ACTIVE PHARMA SCIENCES LIMITED
Effective date: 2026-01-19
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Mebendazole - AX Pharmaceutical Corp \| SOLARA ACTIVE PHARMA SCIENCES LIMITED	AX Pharmaceutical Corp \| SOLARA ACTIVE PHARMA SCIENCES LIMITED	2026-01-19	BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73377-031-01	Mebendazole	100 g in 1 JAR	POWDER	100		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73377-031	MEBENDAZOLE POWDER [AX PHARMACEUTICAL CORP]	1	1 package rows	20200317_35f0eef5-e616-40ac-b4c7-c3a700df8980.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
VERMOX	MEBENDAZOLE	Janssen Pharmaceuticals, Inc.	a720c424-517a-461b-8e13-6c37caf8aa3f	2021-10-05	Warnings, Adverse reactions	Exact identifier unii: 81G6I5V05I

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.